about
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancerDifferential gene expression profile reveals deregulation of pregnancy specific beta1 glycoprotein 9 early during colorectal carcinogenesis.Detectable clonal mosaicism and its relationship to aging and cancerImputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesIdentification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variantsPancreatic cancer genomes reveal aberrations in axon guidance pathway genesA genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancerGenome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancerPMS2 monoallelic mutation carriers: the known unknownDuctal pancreatic cancer modeling and drug screening using human pluripotent stem cell- and patient-derived tumor organoids.A human colon cancer cell capable of initiating tumour growth in immunodeficient miceFemale chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosomeCombined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancersAssociation between biallelic and monoallelic germline MYH gene mutations and colorectal cancer riskThe P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancerCross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic AssociationsIdentification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysisGenome-wide diet-gene interaction analyses for risk of colorectal cancer.Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancerCommon variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer.The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgeryGenes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data.A renewed model of pancreatic cancer evolution based on genomic rearrangement patternsGenetic predisposition to colorectal cancer: new pieces in the pediatric puzzle.Germline EPHB2 receptor variants in familial colorectal cancer.Liver resection after chemotherapy and tumour downsizing in patients with initially unresectable colorectal cancer liver metastases.Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer.Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinicsAdjuvant chemotherapy with fluorouracil plus folinic acid vs gemcitabine following pancreatic cancer resection: a randomized controlled trial.Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers.Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
@en
հետազոտող
@hy
name
Steven Gallinger
@ast
Steven Gallinger
@en
Steven Gallinger
@es
Steven Gallinger
@nl
Steven Gallinger
@sl
type
label
Steven Gallinger
@ast
Steven Gallinger
@en
Steven Gallinger
@es
Steven Gallinger
@nl
Steven Gallinger
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prefLabel
Steven Gallinger
@ast
Steven Gallinger
@en
Steven Gallinger
@es
Steven Gallinger
@nl
Steven Gallinger
@sl